All papers authored by Knut Brockmann
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2023
Simone Schröder,
Gökhan Yigit,
Yun Li,
Janine Altmüller 
,
Hans-Martin Büttel,
Barbara Fiedler,
Christoph Kretzschmar,
Peter Nürnberg,
Jürgen Seeger ,
Valentina Serpieri,
Enza Maria Valente,
Bernd Wollnik,
Eugen Boltshauser,
Knut Brockmann
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,
Hans-Martin Büttel,
Barbara Fiedler,
Christoph Kretzschmar,
Peter Nürnberg,
Jürgen Seeger ,
Valentina Serpieri,
Enza Maria Valente,
Bernd Wollnik,
Eugen Boltshauser,
Knut Brockmann
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2022
Fabian Bockhop ,
Marina Zeldovich ,
Sven Greving ,
Ugne Krenz ,
Katrin Cunitz ,
Dagmar Timmermann,
Elena M. Bonke ,
Michaela V. Bonfert ,
Inga K. Koerte ,
Matthias Kieslich,
Maike Roediger,
Michael Staebler,
Steffen Berweck,
Thomas Paul,
Knut Brockmann
and 3 other authors
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,
Marina Zeldovich ,
Sven Greving ,
Ugne Krenz ,
Katrin Cunitz ,
Dagmar Timmermann,
Elena M. Bonke ,
Michaela V. Bonfert ,
Inga K. Koerte ,
Matthias Kieslich,
Maike Roediger,
Michael Staebler,
Steffen Berweck,
Thomas Paul,
Knut Brockmann
and 3 other authors
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Dagmar Timmermann,
Ugne Krenz ,
Silke Schmidt ,
Michael Lendt,
Christel Salewski ,
Knut Brockmann ,
Nicole von Steinbüchel
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,
Silke Schmidt ,
Michael Lendt,
Christel Salewski ,
Knut Brockmann ,
Nicole von Steinbüchel
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2021
Gökhan Yigit,
Ruth Sheffer,
Muhannad Daana,
Yun Li,
Emrah Kaygusuz,
Hagar Mor-Shakad,
Janine Altmüller ,
Peter Nürnberg,
Liza Douiev,
Silke Kaulfuss,
Peter Burfeind,
Bernd Wollnik ,
Knut Brockmann
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,
Peter Nürnberg,
Liza Douiev,
Silke Kaulfuss,
Peter Burfeind,
Bernd Wollnik ,
Knut Brockmann
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2020
Jan-Henje Döring,
Celina von Stülpnagel,
Afshin Saffari,
Thomas Bast,
Knut Brockmann ,
Laura Ehrhardt,
Walid Fazeli ,
Wibke Gesine Janzarik,
Gerhard Kluger,
Hiltrud Muhle,
Rikke S. Møller ,
Konrad Platzer,
Joana Larupa Santos,
Joana Larupa Santos ,
Iben Bache
and 26 other authors
,
Laura Ehrhardt,
Walid Fazeli ,
Wibke Gesine Janzarik,
Gerhard Kluger,
Hiltrud Muhle,
Rikke S. Møller ,
Konrad Platzer,
Joana Larupa Santos,
Joana Larupa Santos ,
Iben Bache
and 26 other authors
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood
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Simone Schröder,
Yun Li,
Janine Altmüller ,
Ingrid Bader,
Gökhan Yigit,
Andrea Bevot,
Saskia Biskup,
Steffi Dreha-Kulaczewski,
G. Christoph Korenke,
Raimund Kottke ,
Johannes A. Mayr,
Martin Preisel,
Sandra P. Toelle,
Sarah Wente-Schulz,
Eugen Boltshauser
and 5 other authors
,
Ingrid Bader,
Gökhan Yigit,
Andrea Bevot,
Saskia Biskup,
Steffi Dreha-Kulaczewski,
G. Christoph Korenke,
Raimund Kottke ,
Johannes A. Mayr,
Martin Preisel,
Sandra P. Toelle,
Sarah Wente-Schulz,
Eugen Boltshauser
and 5 other authors
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia
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2016
Sarah Wente,
Simone Schröder,
Johannes Buckard,
Hans-Martin Büttel,
Florian von Deimling,
Wilfried Diener,
Martin Häussler,
Susanne Hübschle,
Silvia Kinder,
Gerhard Kurlemann,
Christoph Kretzschmar,
Michael Lingen,
Wiebke Maroske,
Dirk Mundt,
Iciar Sánchez-Albisua
and 4 other authors
Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study
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